CS(=O)(=O)OC1=C(N2[C@H](CC1)[C@H](NC(=O)COC1=CC=CC=C1)C2=O)C(O)=O

InChIKey=SKSQTFBTTUIFLN-RISCZKNCSA-N

C17H18N2O8S

410.4

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Not available

Carbacephems

N-acyl-alpha amino acids and derivatives Phenoxy compounds Phenol ethers Tetrahydropyridines Alkyl aryl ethers Sulfonic acid esters Organosulfonic acid esters Tertiary carboxylic acid amides Sulfonyls Methanesulfonates Tertiary amines Secondary carboxylic acid amides Amino acids Azetidines Monocarboxylic acids and derivatives Azacyclic compounds Carboxylic acids Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteropolycyclic compounds

Carbacephem - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Phenoxy compound - Phenol ether - Alkyl aryl ether - Tetrahydropyridine - Monocyclic benzene moiety - Benzenoid - Organosulfonic acid ester - Sulfonic acid ester - Methanesulfonate - Tertiary carboxylic acid amide - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Amino acid or derivatives - Azetidine - Amino acid - Carboxamide group - Tertiary amine - Secondary carboxylic acid amide - Monocarboxylic acid or derivatives - Ether - Carboxylic acid - Carboxylic acid derivative - Azacycle - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Amine - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as carbacephems. These are a new class of beta-lactam antibiotics similar in structure to the cephalosporins. They differ from cephalosporins, however, in the substitution of a sulfur atom in the dihydrothiazine ring with a methylene group to form a tetrahydropyridine ring.

Not available